[3 + 2] cycloaddition of 1-(4-Methoxybenzyl)indoles and azaindoles with nitrile oxides
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In the [3 + 2] cycloaddition of a range of nitrile oxides with homochiral vinyl ethers the diastereoselectivity observed is dependent on the chiral auxiliary used. A brief comparison is made with the diastereoselectivity of the corresponding [4 + 2] nitrosoalkene cycloaddition, and also to the nitrile oxide cycloaddition to chiral acrylic acid esters bearing the most successful auxiliaries from the vinyl ether study.
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The 1,3-dipolar cycloaddition reaction of nitrile oxides with carbon dipolarophiles is a versatile and powerful synthetic method to prepare isoxazolines. In particular nitrile oxide cycloaddition reactions with exocyclic methylene or alkylidene compounds generally proceed regioselectively leading to spiro heterocyclic compounds. This review deals with progress in the field of nitrile oxide cycloaddition chemistry for the synthesis of spiro isoxazolines. Keywords: Nitrile oxide, dipolar cycloaddition, heterocycle, spiro, exocyclic methylene, isoxazoline
Methylene
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Мaқaлa дипломaтиялық іс-қaғaздaрының коммуникaтивті- прaгмaтикaлық ерекшелікте рін зерттеуге aрнaлғaн. Берілген мaқaлaдa aрaб тіліндегі дипломaтиялық іс қaғaздaрының сипaтты интегрaнттaрын aнықтaу мaқсaтындa aлғaш рет коммуникaтивті- прaгмaтикaлық aнaлиз жaсaлды. Зерттеу дипломaтиялық хaт aлмaс удың лексикaлық және синтaксистік проблемaлaрын aйқындaу негізінде жүргізілді. Зерттеудің қорытындысындa коммуникaтивті- прaгмaтикaлық ерекшеліктің шынaйылығы көрсетілді. Ауызшa нотa жaнрының aқпaрaттaндыру прaгмaтикaсы диплом aтиялық дискурстың қaтысушылaрының (aдресaнт пен aдресaт) кеңістік- уaқыттық өзaрa қaрым-қaтынaстaрын (хронотопты) және тaлқылaнaтын нысaнды aнықтaудaн өз көрінісін тaбaды. Дипломaтиялық дискурстың уaқыт индикaциясындa негізгі рөлді етістік aтқaрaтыны нaқты мысaлдaр aрқылы дәлелденді. Етістіктен бaсқa aуызшa нотaлaрдың мәтінінде уaқытты, күн, aй және жылды көрсету сияқты, нaқты индикaторлaрдың белсенді қолдaнылуы осы жaнрдың институционaлдығын aнықтaйды. Нaқты мерзімдерді (дaтaны – күн, aптa, aй, жылды) көрсету проспективaлық сипaтты, коммуникaнттaрдың өзaрa әрекеттестігін сипaттaйды. Мaқaлaдa прaгмa лингвистикaлық және дискурсивтік тaлдaу тұрғысынaн дипломaтиялық дискурстың лингвопрaгмaтикaлық сипaттaрынa кешенді зерттеу жүргізуге тaлпыныс жaсaлды. Мaқaлa жaзбaшa дипломaтиялық коммуникaциялaрдың дискурсивтік жaнрын лингвистикaлық тaлдaудың aйқын, әрі бaсым нысaны ретіндеболaшaқтa жүргізілетін зерттеулерге бaстaпқы қaдaм болып тaбылaды.
Socialization
Sudden Death
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Abstract A systematic highlight of syntheses reported since 2006 of 1,2,3-triazole-fused macrocycles possessing biological activities such as anticancer, antibacterial, antiviral, anti-inflammatory and antilarval action, is presented in this review. The well-renowned Cu-catalyzed azide-alkyne cycloaddition reaction was noted to be highly efficient and is one the most common methods utilized by scientists for the synthesis of 1,4-disubstituted triazole-fused macrocycles, whereas Ru-catalyzed cycloaddition is common for the formation of 1,5-disubstituted bioactive triazoles. This review would thus be extremely beneficial for both synthetic organic and medicinal chemists. 1 Introduction 2 Anticancer Derivatives 3 Antibacterial Derivatives 4 Derivatives with Dual Activity 5 Antilarval Derivatives 6 Anti-inflammatory Derivatives 7 Antiviral Derivatives 8 Anti-trypanosomal Derivatives 9 Derivatives with Miscellaneous Activities 10 Conclusion
Alkyne
Triazole
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1,3-Dipolar cycloaddition has been employed as a powerful synthetic procedure by which five-membered heterocyclic frameworks are constructed together with forming two bonds in a single manipulation. Among the various functionalized nitrile oxides reported, the ethoxycarbonyl derivative 1 is commonly used in organic synthesis. In this chapter, another generation method for 6 from easily available nitroisoxazolone 10 is introduced, which proceeds under mild conditions without using any special reagents. 2-Methyl-4-nitroisoxazol-5(2H)-one 10 having multifunctionalities reveals versatile reactivity to serve as a precursor for polyfunctionalized systems. The carbamoyl group of the nitrile oxide plays an important role not only as an electron-withdrawing group but also as an accelerator in the cycloaddition by forming a hydrogen bond with a dipolarophilic nitrile. The electron-withdrawing carbamoyl group realizes the cycloaddition with electron-rich dipolarophiles, which is inverse electron-demand 1,3-dipolar cycloaddition.
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Practical and efficient methods have been developed for the diversity-oriented synthesis of isoxazolodihydropyridinones via the 1,3-dipolar cycloaddition of nitrile oxides onto 2,4-dioxopiperidines. A select few of these isoxazolodihydropyridinones were further elaborated with triazoles by copper-catalyzed azide-alkyne cycloaddition reactions. A total of 70 compounds and intermediates were synthesized and analyzed for drug likeness. Sixty-four of these novel compounds were submitted to the NIH Molecular Libraries Small Molecule Repository for high-throughput biological screening.
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The involvement of 1,3-dipolar cycloaddition (1,3-DP), double bond migration, metathesis, and nitrile oxide (including in situ-generated nitrile oxide) as dipoles, together with the C=C bond containing dipolarophiles, in the syntheses of 2-isoxazolines is presented. Methods for synthesizing isoxazolines (other than 1,3-DP cycloaddition) were also presented briefly. Various methods of nitrile oxide preparation, especially in situ-generated procedures, are presented. Special attention was paid to the application of various combinations of 1,3-DP cycloaddition with double bond migration (DBM) and with alkene metathesis (AM) in the syntheses of trisubstituted isoxazolines. Allyl compounds of the type QCH2CH=CH2 (Q = ArO, ArS, Ar, and others) play the role of dipolarophile precursors in the combinations of DPC mentioned, DBM and AM. Mechanistic aspects of cycloadditions, i.e., concerted or stepwise reaction mechanism and their regio- and stereoselectivity are also discussed from experimental and theoretical points of view. Side reactions accompanying cycloaddition, especially nitrile oxide dimerization, are considered. 2-Isoxazoline applications in organic synthesis and their biological activity, broad utility in medicine, agriculture, and other fields were also raised. Some remaining challenges in the field of 1,3-DP cycloaddition in the syntheses of isoxazolines are finally discussed.
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